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Áã Çظ¶ÀÇ Lipopolysaccharide ±¹¼ÒÁÖÀÔ¿¡ ÀÇÇÑ Tumor Necrosis Factor-¥á, Interleukin-1¥â ¹× Inducible Nitric Oxide SynthaseÀÇ ¹ßÇö Expression of Tumor Necrosis Factor-¥á, Interleukin-1¥â and Inducible Nitric Oxide Synthase after Stereotaxic Injection of Lipopolysaccharide in Rat Hippocampus

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¿ÀÈƱԠ( Oh Hoon-Kyu ) 
´ë±¸°¡Å縯´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç

¹ÚÁö¿µ ( Park Ji-Young ) 
¼º±Õ°ü´ëÇб³ ÀÇ°ú´ëÇÐ »ï¼ºÁ¦ÀϺ´¿ø º´¸®°ú
°­±¸¼º ( Kang Ku-Seong ) 
°æºÏ´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
±èÁ¤¿Ï ( Kim Jung-Wan ) 
°æºÏ´ëÇб³ Ä¡°ú´ëÇÐ ±¸°­¹Ì»ý¹°Çб³½Ç
¼ÕÀ±°æ ( Sohn Yoon-Kyung ) 
°æºÏ´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
°ûÀº°æ ( Kwak Eun-Kyoung ) 
°æºÏ´ëÇб³ Ä¡°ú´ëÇÐ ±¸°­º´¸®Çб³½Ç
±èÁö¿¬ ( Kim Ji-Yeon ) 
°æºÏ´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç

Abstract


Background:inducible nitric oxide synthase (iNOS) might be detectable in several pathologic conditions, and it is thought to play an important role in their pathophysiology. Tumor necrosis factor (TNF)-¥á and interleukin (IL)-1¥â are believed to be essential factors of iNOS induction of the brain.

mothods: After intrahippocampal stereotaxic injection of lipopoly-saccharide (LPS), the rat brains were removed at 6, 12 and 24 h. The rat brain tissues were examined to clarify the expression patterns of TNF-¥á, IL-1¥â and iNOS.

Results: The inflammatory cells which were stained with anti-TNF-¥á antibody, appeared in 6 h and increased for 24 h after LPS injection. The iNOS positive cells appeared after 12 h of LPS injection. A semiquantitative analysis of reverse transcription-polymerase chain reaction (RT-PCR) revealed that the TNF-¥á and IL-1¥â mRNA arose at 1 h, peaked at 6 h and then declined until 48 h after LPS injection. The iNOS mRNA arose after 6 h, peaked at 12 h, and declined until 48 h after LPS injection.

Conclusions: We conclude that the induction of inflammatory events by intrahippocampal injection of LPS activates TNF-¥á and IL-1¥â secretion, and this is followed by an induction of iNOS expression. TNF-¥á and IL-1¥â seem to be related with iNOS expression in brain inflammation.

Å°¿öµå

Inducible Nitric Oxide Synthase;Tumor Necrosis Factor;Interleukins;Lipopoly;saccharides;Hippocampus

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